Cargando…
Predicting growth of the healthy infant using a genome scale metabolic model
An estimated 165 million children globally have stunted growth, and extensive growth data are available. Genome scale metabolic models allow the simulation of molecular flux over each metabolic enzyme, and are well adapted to analyze biological systems. We used a human genome scale metabolic model t...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460126/ https://www.ncbi.nlm.nih.gov/pubmed/28649430 http://dx.doi.org/10.1038/s41540-017-0004-5 |
_version_ | 1783242099947208704 |
---|---|
author | Nilsson, Avlant Mardinoglu, Adil Nielsen, Jens |
author_facet | Nilsson, Avlant Mardinoglu, Adil Nielsen, Jens |
author_sort | Nilsson, Avlant |
collection | PubMed |
description | An estimated 165 million children globally have stunted growth, and extensive growth data are available. Genome scale metabolic models allow the simulation of molecular flux over each metabolic enzyme, and are well adapted to analyze biological systems. We used a human genome scale metabolic model to simulate the mechanisms of growth and integrate data about breast-milk intake and composition with the infant’s biomass and energy expenditure of major organs. The model predicted daily metabolic fluxes from birth to age 6 months, and accurately reproduced standard growth curves and changes in body composition. The model corroborates the finding that essential amino and fatty acids do not limit growth, but that energy is the main growth limiting factor. Disruptions to the supply and demand of energy markedly affected the predicted growth, indicating that elevated energy expenditure may be detrimental. The model was used to simulate the metabolic effect of mineral deficiencies, and showed the greatest growth reduction for deficiencies in copper, iron, and magnesium ions which affect energy production through oxidative phosphorylation. The model and simulation method were integrated to a platform and shared with the research community. The growth model constitutes another step towards the complete representation of human metabolism, and may further help improve the understanding of the mechanisms underlying stunting. |
format | Online Article Text |
id | pubmed-5460126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54601262017-06-23 Predicting growth of the healthy infant using a genome scale metabolic model Nilsson, Avlant Mardinoglu, Adil Nielsen, Jens NPJ Syst Biol Appl Article An estimated 165 million children globally have stunted growth, and extensive growth data are available. Genome scale metabolic models allow the simulation of molecular flux over each metabolic enzyme, and are well adapted to analyze biological systems. We used a human genome scale metabolic model to simulate the mechanisms of growth and integrate data about breast-milk intake and composition with the infant’s biomass and energy expenditure of major organs. The model predicted daily metabolic fluxes from birth to age 6 months, and accurately reproduced standard growth curves and changes in body composition. The model corroborates the finding that essential amino and fatty acids do not limit growth, but that energy is the main growth limiting factor. Disruptions to the supply and demand of energy markedly affected the predicted growth, indicating that elevated energy expenditure may be detrimental. The model was used to simulate the metabolic effect of mineral deficiencies, and showed the greatest growth reduction for deficiencies in copper, iron, and magnesium ions which affect energy production through oxidative phosphorylation. The model and simulation method were integrated to a platform and shared with the research community. The growth model constitutes another step towards the complete representation of human metabolism, and may further help improve the understanding of the mechanisms underlying stunting. Nature Publishing Group UK 2017-01-31 /pmc/articles/PMC5460126/ /pubmed/28649430 http://dx.doi.org/10.1038/s41540-017-0004-5 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Nilsson, Avlant Mardinoglu, Adil Nielsen, Jens Predicting growth of the healthy infant using a genome scale metabolic model |
title | Predicting growth of the healthy infant using a genome scale metabolic model |
title_full | Predicting growth of the healthy infant using a genome scale metabolic model |
title_fullStr | Predicting growth of the healthy infant using a genome scale metabolic model |
title_full_unstemmed | Predicting growth of the healthy infant using a genome scale metabolic model |
title_short | Predicting growth of the healthy infant using a genome scale metabolic model |
title_sort | predicting growth of the healthy infant using a genome scale metabolic model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460126/ https://www.ncbi.nlm.nih.gov/pubmed/28649430 http://dx.doi.org/10.1038/s41540-017-0004-5 |
work_keys_str_mv | AT nilssonavlant predictinggrowthofthehealthyinfantusingagenomescalemetabolicmodel AT mardinogluadil predictinggrowthofthehealthyinfantusingagenomescalemetabolicmodel AT nielsenjens predictinggrowthofthehealthyinfantusingagenomescalemetabolicmodel |